AQUACOOL MULTI ROLL

Product NDC
70759-0010
11-digit product format
707590010
Labeler code
70759
Product ID
70759-0010_bd2824d1-76d5-2af7-e053-2995a90a3177
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Pharmanuco
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-12-01
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
3 g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70759-0010-12022-07-29C16284748780-1ba0f9c33-2ccd-a910-e053-dadaa90a0b85Drug Facts
70759-0010-12021-03-10C16284748780-1ba0f9c33-2ccd-a910-e053-dadaa90a0b85Drug Facts
70759-0010-12021-01-29C16284748780-1ba0f9c33-2ccd-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70759-0010-1AQUACOOL MULTI ROLL100 mL in 1 BOTTLE, WITH APPLICATORGEL1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70759-0010AQUACOOL MULTI ROLL (MENTHOL) GEL [PHARMANUCO]2Legacy NDC, 1 package rows20210311_60d116e1-d0e8-297a-e053-2a91aa0a1a4c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
259150menthol 3 % Topical GelPSN60d116e1-d0e8-297a-e053-2a91aa0a1a4c2
259150menthol 0.03 MG/MG Topical GelSCD60d116e1-d0e8-297a-e053-2a91aa0a1a4c2
259150menthol 3 % Topical GelSY60d116e1-d0e8-297a-e053-2a91aa0a1a4c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70759-0010-170759001001100 mL in 1 BOTTLE, WITH APPLICATOR (70759-0010-1) 100 ml2017-12-010000-00-00NoNoCurrent